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【结 构 式】

【分子编号】54980

【品名】(8S,9S,12S,13R,14S,16R)-13-hydroxy-8,14,19-trimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate

【CA登记号】

【 分 子 式 】C29H40N2O9

【 分 子 量 】560.64468

【元素组成】C 62.13% H 7.19% N 5% O 25.68%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(I)

The title compound was prepared by displacement of the 17-methoxy group of geldanamycin (I) with allylamine (II) in chloroform at room temperature.

1 Schnur, R.C.; et al.; erbB-2 oncogene inhibition by geldanamycin derivatives: Synthesis, mechanism of action, and structure-activity relationships. J Med Chem 1995, 38, 19, 3813.
2 Inoue, Y.; Sasaki, K. (Kaken Pharmaceutical Co., Ltd.); Geldanamycin derivs. and antitumor drug. US 4261989 .
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 54980 (8S,9S,12S,13R,14S,16R)-13-hydroxy-8,14,19-trimethoxy-4,10,12,16-tetramethyl-3,20,22-trioxo-2-azabicyclo[16.3.1]docosa-1(21),4,6,10,18-pentaen-9-yl carbamate C29H40N2O9 详情 详情
(II) 13672 Allylamine; 2-Propen-1-amine 107-11-9 C3H7N 详情 详情
Extended Information